Wilson C A, Eiden M V, Marsh J W
Laboratory of Cell Biology, National Institute of Mental Health, Bethesda, MD 20892.
J Virol Methods. 1994 Jun;48(1):109-17. doi: 10.1016/0166-0934(94)90093-0.
An anti-P30 immunohistochemical and a reverse transcriptase assay for Moloney murine leukemia virus (MoMLV) are adapted to 96-well plates. The assay results are shown to be directly proportional to the number of infectious particles, and can therefore be used to estimate the infective titers of a virus preparation. The micro P30 assay yields a direct estimate of infectious centers, and the reverse transcriptase assay quantitates progeny from a single cycle of replication. The semi-automated nature of these assays is well suited to the analysis of a large number of samples and therefore permits the examination of the efficiency of the process of retroviral/MoMLV infection under varied times or conditions.
针对莫洛尼鼠白血病病毒(MoMLV)的抗P30免疫组织化学检测和逆转录酶检测被应用于96孔板。检测结果显示与感染性颗粒的数量成正比,因此可用于估算病毒制剂的感染滴度。微量P30检测可直接估算感染中心,逆转录酶检测可对单个复制周期产生的子代进行定量。这些检测的半自动特性非常适合分析大量样本,因此可以在不同时间或条件下检测逆转录病毒/MoMLV感染过程的效率。